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How much do clinical research educator jobs pay per hour?

As of Sep 15, 2026, the average hourly pay for clinical research educator in the United States is $43.95, according to ZipRecruiter salary data. Most workers in this role earn between $33.65 and $52.40 per hour, depending on experience, location, and employer.

What is a clinical research educator?

A Clinical Research Educator is a professional who develops, implements, and delivers educational programs related to clinical research for healthcare staff, research teams, and sometimes patients. They ensure that all involved parties are informed about the latest protocols, regulatory requirements, and best practices in clinical trials. Their work helps improve the quality, safety, and compliance of clinical research activities within healthcare organizations.

How does a clinical research educator collaborate with research teams to enhance study protocol adherence?

Clinical Research Educators play a key role in bridging the gap between research protocols and practical implementation. They work closely with investigators, study coordinators, and healthcare staff to provide targeted training, clarify regulatory requirements, and address protocol-specific challenges. By facilitating workshops, creating educational materials, and offering one-on-one support, they help ensure that all team members understand and consistently follow study procedures, ultimately supporting high-quality research outcomes.

What are the key skills and qualifications needed to thrive as a clinical research educator, and why are they important?

To thrive as a Clinical Research Educator, you need a strong background in clinical research methodologies, regulatory compliance, and adult education, often supported by a degree in life sciences or nursing and experience in research settings. Familiarity with research management systems, electronic data capture (EDC) tools, and certifications such as CCRA or CCRC are highly beneficial. Excellent communication, presentation, and interpersonal skills help engage learners and foster collaboration among multidisciplinary teams. These competencies ensure accurate knowledge transfer, regulatory adherence, and the development of skilled clinical research professionals.

What is the difference between Clinical Research Educator vs Clinical Research Coordinator?

AspectClinical Research EducatorClinical Research Coordinator
Required CredentialsBachelor's degree, certifications in clinical research (e.g., CCRP)Bachelor's degree, often certifications in clinical research or related fields
Work EnvironmentEducational settings, training programs, industry seminarsHospitals, clinics, research sites
Employer & Industry UsagePharmaceutical companies, research institutions, training organizationsAcademic medical centers, hospitals, research sites
Common Search & ComparisonYesYes

The Clinical Research Educator primarily focuses on training and educating staff or students about clinical research protocols, regulations, and best practices. In contrast, the Clinical Research Coordinator manages the day-to-day operations of clinical trials at research sites. While both roles require similar certifications and work within the clinical research industry, their core responsibilities and work environments differ significantly.

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What are popular job titles related to Clinical Research Educator jobs?

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Clinical Research Educator jobs near you
Infographic showing various Clinical Research Educator job openings in the United States as of August 2026, with employment types broken down into 4% As Needed, 70% Full Time, 17% Part Time, and 9% Contract. Highlights an 94% Physical, 1% Hybrid, and 5% Remote job distribution, with an average salary of $91,418 per year, or $44 per hour.

Clinical Research Coordinator

Freehold, NJ • On-site

Tandem Clinical Research
Scientific Research and Development Services • 11 - 50 employees
Learn more about Tandem Clinical Researchexternal

$24.25 - $32.25/hr

Full-time

Posted 4 days ago

Job description

Clinical Research Coordinator (CRC)
The Clinical Research Coordinator (CRC) is responsible for overseeing and managing the daily operational activities of assigned clinical research studies. This role works closely with investigators, clinical staff, study participants, sponsors, and CROs to ensure that all research activities are conducted in compliance with study protocols, regulatory requirements, and ethical standards.
The CRC serves as the primary owner of study coordination, documentation, data management, and sponsor communication, supporting compliant trial execution from study start-up through close-out.
Key Responsibilities
Study Management & Coordination
  • Organize, plan, and coordinate all aspects of assigned clinical trials from initiation through close-out.
  • Support study start-up activities including feasibility, regulatory submissions, and site activation.
  • Attend investigator meetings, site initiation visits, and other study-related meetings.
  • Manage visit schedules and coordinate study-related activities across clinical teams.

Recruitment, Enrollment & Consent
  • Collaborate with recruitment teams to support participant screening and enrollment.
  • Conduct informed consent discussions with participants, ensuring understanding of study requirements and documentation of consent.
  • Ensure protocol and regulatory requirements are met throughout the enrollment process.

Clinical Oversight & Subject Monitoring
  • Monitor and assess study subjects in accordance with protocol requirements.
  • Identify, document, and report adverse events in collaboration with the Principal Investigator and clinical staff.
  • Escalate safety concerns and protocol issues to the PI, sponsor, and IRB as required.

Documentation, Data & Systems
  • Maintain accurate and complete source documentation, case report forms, regulatory files, and study records.
  • Enter study data into EDC and other required systems and manage study databases.
  • Complete, verify, and resolve case report forms and sponsor or monitor queries in a timely manner.
  • Report protocol deviations to the PI, sponsor, and IRB as required.

Investigational Product & Specimen Management
  • Manage investigational product accountability records and documentation.
  • Collect, process, package, and ship study specimens per protocol requirements.
  • Perform phlebotomy and handle biological specimens in accordance with study protocols and safety guidelines, when trained and authorized.

Quality, Compliance & Team Support
  • Ensure all study activities comply with SOPs, GCP, and regulatory requirements.
  • Support quality assurance activities and audit readiness.
  • Provide assistance and mentorship to fellow coordinators as needed.
  • Maintain strict confidentiality of participant and study information.

Communication & Outreach
  • Serve as the primary point of contact for sponsor and CRO communications.
  • Participate in occasional outreach or community events related to clinical trials.
  • Ensure timely, accurate communication of study updates and issues.

Additional Responsibilities
This job description outlines the primary responsibilities of the Clinical Research Coordinator but is not exhaustive. Additional duties may be assigned as needed to support study requirements, operational needs, and organizational priorities. Responsibilities may evolve based on protocol complexity and business needs.
Requirements
  • Knowledge, Skills, and Abilities
  • Strong leadership and communication skills
  • Exceptional organizational and multitasking abilities
  • High attention to detail and commitment to regulatory compliance
  • Ability to work independently and collaboratively in a multidisciplinary environment
  • Strong time management and operational efficiency skills
  • Proficiency with office equipment and study-specific systems
  • Ability to maintain strict confidentiality
  • Required Experience & Qualifications
  • Education: Bachelor's degree in a related field
  • Experience: Minimum of two (2) years of clinical research or clinical trial management experience
  • Preferred Credentials: Medical certification or licensure (e.g., MS, LPN, RN)
  • Phlebotomy: Prior experience performing blood draws and handling biological specimens required

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